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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1908229Erstellt: 23. Oktober 2026

Methanol → alpha-(Aminomethyl)-3,4-dichlorobenzenemethanol

https://huagongshe.com/de/reaction/1908229

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt3,4-DichlorobenzaldehydeHCID 22710—
EduktTrimethylsilyl cyanideHCID 82115—
EduktBorane;tetrahydrofuranHCID 2723981—
Katalysatorzinc(II)iodideHCID 9883512—
LösungsmittelTetrahydrofuranHCID 8028—
Produktalpha-(Aminomethyl)-3,4-dichlorobenzenemethanolHCID 19349772%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a mixture of 3,4-dichlorobenzaldehyde (3.50 g, 20.2 mmol) and ZnI2 (19 mg, 0.06 mmol) at 0° C. was added TMSCN (2.2 g, 2.2 mmol). The reaction mixture was stirred at 0° C. for 10 min and then warmed to rt and stirred for an additional 1 h. The mixture was concentrated to afford an orange-brown colored oil. The oil was dissolved in THF (20 mL) and BH3.THF (1 M in THF; 25 mL, 25 mmol) was added at 0° C. The reaction mixture was warmed to rt and stirred overnight. The mixture was cooled to 0° C. and MeOH (6 mL) was added with continued stirring for 2 h. After being warmed to rt, the mixture was concentrated. The residue was dissolved in MeOH (10 mL) and HCl (2 M in Et2O; 25 mL) was added at 0° C. After 30 min, Et2O (100 mL) was added and the resulting white solid was filtered and washed with Et2O (2×50 mL) to give a white solid (3.5 g, 72%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08598202B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-0689aa7f7264494d988f565bb322fb78
Quellennotizuspto-grants-2013_12